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High Resolution Image Download MS PowerPoint Slide The luminescent quantum yield of silver-cluster emitters stabilized by short oligonucleotides (Ag N -DNA) may be efficiently tuned by replacing nucleobases in their stabilization DNA matrices with analogues. In the present study, we proposed a valuable and straightforward theoretical methodology for assessing the photophysical behaviors emerging in Ag N -DNA emitters after excitation. Using green Ag 10 -DNA and near-IR Ag 16 -DNA emitters we demonstrate how point guanine/inosine replacement could affect the photophysical rate constants of radiative/nonradiative processes. The main deactivation channel of the fluorescence of Ag 16 -DNA is intersystem crossing, which is in line with experimental data, whereas for Ag 10 -DNA the calculations overestimate the intersystem crossing rate possibly due to pure solvent contributions.
Ramazanov et al. (2024) studied this question.